GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glcE in Desulfovibrio vulgaris Hildenborough

Align D-lactate oxidase, FAD binding subunit (EC 1.1.3.15) (characterized)
to candidate 209326 DVU0390 glycolate oxidase, subunit GlcD, putative

Query= reanno::Cup4G11:RR42_RS17310
         (374 letters)



>MicrobesOnline__882:209326
          Length = 460

 Score = 79.0 bits (193), Expect = 3e-19
 Identities = 111/411 (27%), Positives = 164/411 (39%), Gaps = 69/411 (16%)

Query: 19  IRHATGTRTPLRLRGGGSKDFYG--QHPQGTLLDTRAYSGIVDYDPPELV--ITARCGTP 74
           +R AT  R P+  RGGG+    G      G +L     + +   D   LV  + A C T 
Sbjct: 60  MRLATEHRFPVIPRGGGTGLAGGCLALMGGVVLSVERMNRVRAIDTRNLVAEVDAGCITQ 119

Query: 75  LAQIEAALAERRQMLAFEPPHFSTGADGSDVATIGGAVAAGLSGPRRQAVGALRDFVLGT 134
             +  AA A       F PP  +    G D +T+GG VA    GP     G  RD+VLG 
Sbjct: 120 TLRDAAAAAN-----LFYPPDPA----GMDRSTVGGNVATNAGGPACVKYGVTRDYVLGV 170

Query: 135 RVMDGRGDVLSFGGQVMKNVAGYDVSRLMSGSLGTLGLILEVSLKVLPVPFDDATLRFAL 194
             +   G++L  G +  K V GYD++ L+ GS GTLG+I  +++K++P+P     +  A 
Sbjct: 171 EAVLPDGELLRAGVRTRKGVVGYDMAHLLCGSEGTLGVITGLTMKLIPLPAATVGMAVAF 230

Query: 195 DEAAALDR--LNDWGGQPLPIAASAWHDGVLHLRLSGAAAALRAARARL------GGEAV 246
            +  +  R      G   LP A        L L        +  AR  L      G  A 
Sbjct: 231 ADMPSAMRAVAAVLGAGHLPSAIEFMDHRCLALVGEMLPFPVPGARPSLLIIELDGQRAT 290

Query: 247 DAAQADALWRALREH--SHAFFAPVQAGRA-LW--------------------RIAVPTT 283
              Q DA+    RE   +    AP  A RA +W                     +AVP  
Sbjct: 291 IEPQLDAVAAICREQGATQVLPAPTDAERATIWGVRRQVSLRIHDYAGLYLSEDVAVPLV 350

Query: 284 AAP---LALP------GGQLIEWG--GGQRWWLGGSDSAADS------AIVRAAAKAAGG 326
           A       LP      G ++  +G  G     L  + S+ D+       +V  A +    
Sbjct: 351 AIADLVAELPAFEERYGLEIFAFGHAGDGNIHLNVTSSSTDNRERAEEGVVALARRVVEL 410

Query: 327 HATLFRNGDKAVG------VFTPLSAPVAAIHQRLKATFDPAGIFNPQRMY 371
             T+  +G+  +G      V   LSA   A+ + ++  FDP GI NP +++
Sbjct: 411 GGTI--SGEHGIGEAKKHLVPLELSARSIALQKGIRGVFDPLGIMNPGKVF 459


Lambda     K      H
   0.321    0.136    0.414 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 387
Number of extensions: 23
Number of successful extensions: 2
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 374
Length of database: 460
Length adjustment: 31
Effective length of query: 343
Effective length of database: 429
Effective search space:   147147
Effective search space used:   147147
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory